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CAS 206257-39-8

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Ethyl 6-bromo-4-chloroquinoline-3-carboxylate

Description:
Ethyl 6-bromo-4-chloroquinoline-3-carboxylate is a chemical compound belonging to the quinoline family, characterized by its fused bicyclic structure that includes a nitrogen atom. This compound features a carboxylate ester functional group, which contributes to its reactivity and solubility properties. The presence of bromine and chlorine substituents on the quinoline ring enhances its potential for various chemical reactions, including electrophilic aromatic substitution. Ethyl 6-bromo-4-chloroquinoline-3-carboxylate is typically used in organic synthesis and medicinal chemistry, where it may serve as an intermediate in the development of pharmaceuticals or agrochemicals. Its molecular structure allows for potential interactions with biological targets, making it of interest in drug discovery. Additionally, the compound's physical properties, such as melting point, boiling point, and solubility, can vary based on the specific conditions and solvents used. Safety data should be consulted to handle this compound appropriately, as halogenated compounds can exhibit toxicity and environmental concerns.
Formula:C12H9BrClNO2
InChI:InChI=1/C12H9BrClNO2/c1-2-17-12(16)9-6-15-10-4-3-7(13)5-8(10)11(9)14/h3-6H,2H2,1H3
SMILES:CCOC(=O)c1cnc2ccc(cc2c1Cl)Br
Synonyms:
  • 3-Quinolinecarboxylic Acid, 6-Bromo-4-Chloro-, Ethyl Ester
  • Ethyl 6-bromo-4-chloro-3-quinolinecarboxylate
  • Ethyl6-bromo-4-chloroquinoline-3-carboxylate,97%
  • 6-BROMO-4-CHLORO-QUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER
  • UKRORGSYN-BB BBV-080772
  • 6-Bromo-4-chloro-3-quinolinecarboxylic acid ethyl ester
  • ETHYL 6-BROMO-4-CHLORO-3-QUINOLINECARBOXYLATE-4
  • EOS-60328
  • Ethyl4-chloro-6-bromoquinoline-3-carboxylate
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